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The first case of a complete deficiency of diphosphoglycerate mutase in human erythrocytes.

An inherited and complete deficiency of diphosphoglycerate mutase was discovered in the erythrocytes of a 42-yr-old man of French origin whose blood hemoglobin concentration was 19.0 g/dl. Upon physical examination he was normal with the exception of a ruddy cyanosis. The morphology of his erythrocy...

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Bibliografske podrobnosti
izdano v:J Clin Invest
Main Authors: Rosa, R, Prehu, M O, Beuzard, Y, Rosa, J
Format: Artigo
Jezik:Inglês
Izdano: American Society for Clinical Investigation 1978
Teme:
Online dostop:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC371847/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/152321/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI109218
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